NCT06691529

Brief Summary

The association of metabolic associated fatty liver disease in patients with chronic glomerular disease

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2024

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 14, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 15, 2024

Completed
16 days until next milestone

Study Start

First participant enrolled

December 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

November 18, 2024

Status Verified

November 1, 2024

Enrollment Period

1 year

First QC Date

November 14, 2024

Last Update Submit

November 15, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • association between metabolic associated fatty liver disease and chronic kidney disease

    To detect the association between metabolic associated fatty liver disease and chronic kidney disease with glomerular diseaese in Assuit university hospital.

    through study completion, an average of 1 year

Study Arms (1)

study group

500 patients presented at Nephrology unit/Internal Medicine department (Assiut University Hospital) In the period 2024-2026.

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients in this study will be subjected to 1. Detailed history and full clinical examination 2. Anthropometric measurements; Hight, weight, waist circumference. 3. Full lab investigations (Complete blood picture , kidney function tests, liver function tests, serum electrolytes, Ferritin, Uric acid level, Prothrombin time and concentration and serum albumin) 4. High sensitivity CRP 5. lipid profile (Fasting) 6. urine analysis, ACR. 7. Available documented renal biopsy 8. HBA1c 9. C- peptide levels. 10. FIB4 - score

You may qualify if:

  • All CKD patient aging between (18-70) years with known tubule-glomerular diseases.
  • At any eGFR.
  • All CKD patient have either type I/II DM associated with CKD .

You may not qualify if:

  • CKD patients of Unknown etiology.
  • CKD patients with liver cirrhosis.
  • CKD patients secondry to documented diabetic nephropathy.
  • Patients with previous/current HBV or HCV.
  • Pregnant CKD patients.
  • Patient commencing any hepatotoxic medication.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Non-alcoholic Fatty Liver Disease

Condition Hierarchy (Ancestors)

Fatty LiverLiver DiseasesDigestive System Diseases

Central Study Contacts

Samar Fahmy Amin

CONTACT

Hussein Ahmed El_Amin

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
physician

Study Record Dates

First Submitted

November 14, 2024

First Posted

November 15, 2024

Study Start

December 1, 2024

Primary Completion

December 1, 2025

Study Completion

March 1, 2026

Last Updated

November 18, 2024

Record last verified: 2024-11